- Research article
- Open Access
Reticulate evolution in stick insects: the case of Clonopsis (Insecta Phasmida)
© Milani et al; licensee BioMed Central Ltd. 2010
Received: 26 February 2010
Accepted: 25 August 2010
Published: 25 August 2010
Phasmids show noteworthy abilities to overcome species-specific reproductive isolation mechanisms, including hybridization, polyploidy, parthenogenesis, hybridogenesis and androgenesis. From an evolutionary standpoint, such tangled reproductive interactions lead to the complex phyletic relationships known as "reticulate evolution". Moroccan stick insects of the genus Clonopsis include one bisexual (C. felicitatis) and two closely related parthenogenetic forms (C. gallica, C. soumiae), which represent a polyploid series in chromosome number, but with apparent diploid karyotypes. Moreover, two Clonopsis strains of ameiotic males have been described, C. androgenes-35 and C. androgenes-53. As a consequence, Clonopsis stick insects may have experienced complex micro-evolutionary events, which we try to disentangle in this study.
Mitochondrial cox2 analysis supports a recent divergence of Clonopsis, while AFLPs evidence genetic differentiation not linked to karyotypes, so that parthenogenetic C. gallica and C. soumiae appear to be a mix of strains of polyphyletic origin rather than single parthenogenetic species. Moreover, an admixed hybrid origin seems to be confirmed for C. androgenes.
On the whole, Clonopsis is an intriguing case of reticulate evolution. Actually, complex cladogenetic events should be taken into account to explain the observed genetic structure, including diploidization of polyploid karyotypes, possibly coupled with hybridization and androgenesis. We also proposed a "working hypothesis" to account for the observed data, which deserves further studies, but fits the observed data very well.
Gene duplication, by which identical copies of genes are created within a single genome, is a major evolutionary process in producing new functions in eukaryotes. Among the possible mechanisms to gain extra copies of genes, whole genome duplication has been suggested as an important step in the production of evolutionary novelties, such as in Vertebrates, Arabidopsis and other eukaryotes (see [1, 2] for reviews). In such lineages, ancient polyploidization events have been suggested, followed by a process of diploidization of the genome (i.e. the evolutionary process whereby a polyploid species 'decays' to become diploid; ). Polyploidy is a common feature of stick insects (Phasmida), so they might be a system of choice to study many aspects of polyploidization. Phasmids also show a noteworthy ability to overcome species-specific reproductive isolation mechanisms, so that hybrids are often found . Such hybrids may show high levels of heterozigosity, which, particularly when co-occurring with polyploidy, may allow them to persist for a long time (i.e. their allelic richness would permit better adaptation to changing environments). Hybridization leads also to parthenogenesis, and parthenogenetic females may not be completely isolated from the closest taxa, since backcrosses to paternal or related species may occur to incorporate additional genomes, thus increasing ploidy level and overall genetic variability [4–6]. From an evolutionary standpoint, such tangled reproductive interactions lead to the complex phyletic relationships known as "reticulate evolution" .
To make reticulate evolution of phasmids even more complicated, stick insects may also reproduce by androgenesis, as first discovered in Bacillus hybrids  and recently proposed to account for Leptynia attenuata fast chromosome evolution, as well as for the origin of Pijnackeria hispanica (formerly Leptynia) parthenogens [4, 6, 8].
Another intriguing cytological feature of Phasmida is their extreme karyotype diversity and their capability for deep chromosomal repatterning [8–11]. Moreover, in parthenogenetic forms the chromosome number is extremely variable, and up to 100 can be found .
This paper deals with the molecular characterization of the stick insect genus Clonopsis, focusing on North African strains. The genus included two bisexual North African species, Clonopsis maroccana Bullini & Nascetti (cn = 22/21, XX/X0) and Clonopsis algerica Pantel (cn = 32/31, XX/X0), and an obligate parthenogenetic species, Clonopsis gallica Charpentier, with a wide distribution in North Africa and Europe, showing a karyotype of 54 - 57 chromosomes. Recent studies on Moroccan samples revealed the existence of two additional North African taxa related to C. gallica: the bisexual Clonopsis felicitatis Scali & Milani (cn = 36/35, XX/X0) and the all-female Clonopsis soumiae Scali & Milani (cn = 72) . Together with C. gallica, they form a numerically polyploid series with haploid number n = 18, being C. felicitatis diploid (cn = 36), C. gallica triploid (cn = 54) and C. soumiae tetraploid (cn = 72). Quite surprisingly however, they all seem to be diploid by standard karyotyping techniques (see  for detailed pictures of the karyotypes), so diploidization was considered for these forms, like for the sexual and parthenogenetic stick insect Sipylodea nelida [5, 10]. Furthermore, two strains of ameiotic males, C. androgenes-35 and C. androgenes-53, with cn = 35 (X0) or 53 (X0) diploid karyotypes were found, which, it is suggested, maintain themselves as clonal androgens: these are thought to derive from diploid species hybrids, which, by skipping meiosis, may produce unreduced but genetically and chromosomally balanced sperm, thus becoming able to father clonal sons when inseminating the eggs of the syntopic all-female C. soumiae by excluding its genetic contribution .
With such a complex array of unusual reproduction modes, the genus Clonopsis represents an intriguing system to study reticulate evolution. Since the whole genome sequence of those insects is not available at the moment, we used a more 'classic' approach to their characterization. Previous papers on phasmids showed that the combined use of nuclear and mitochondrial markers may give significant results, therefore, to understand Clonopsis micro-evolution we used the mitochondrial cytochrome oxidase subunit 2 (cox2) and AFLP markers. The cox2 gene has been sequenced over a wide variety of phasmid taxa and has proved useful for phylogenetic research [4, 8, 14], while AFLPs, since their introduction in 1995 , have been successfully used on a large number of organisms, bringing key answers to major biological issues , and have been used to characterize the stick insect genus Timema . As a matter of fact, studies have demonstrated that AFLPs have the capacity to resolve extremely small genetic differences [18, 19], so they have been proposed as the best markers to show up population genetic variability, when compared to other available molecular approaches, such as microsatellites, multigene DNA sequencing and SNPs . AFLPs have also proved to be a very powerful tool for the identification of interspecific and intraspecific hybrids , even in systems where microsatellites have failed to do so . For all the above mentioned reasons, AFLPs seem to be a good choice for unraveling Clonopsis population structure and to obtain data that might eventually shed light on the role of diploidization in their evolution.
Our data suggest that parthenogenetic C. gallica and C. soumiae are a mix of strains of polyphyletic origin rather than single parthenogenetic species, all of them supposedly diploid. To account for this, we discuss Clonopsis reticulate evolution in the light of the known mechanisms of karyotype diploidization. Finally, we propose a testable hypothesis for Clonopsis micro-evolution, which has the merit of fitting in with our data. Of course, our scenario for Clonopsis deserves more in-depth analyses to be tried, nevertheless we feel that this is a sound "working hypothesis".
Collecting sites and acronyms of analyzed Clonopsis specimens.
C. felicitatis (cn = 36/35, XX/X0)
C. gallica (cn = 54)
Oued Laou Area (OLA)
C. gallica (cn = 54)
C. soumiae (cn = 72)
C. soumiae (cn = 72)
C. gallica (cn = 54)
C. soumiae (cn = 72)
C. androgenes-35 (cn = 35)
C. androgenes-53 (cn = 53)
C. androgenes-53 (cn = 53)
C. maroccana (cn = 22/21, XX/X0)
C. gallica (cn = 54-57)
El Bosque (GEL)
C. gallica (cn = 54-57)
C. gallica (cn = 54-57)
C. gallica (cn = 54-57)
Paterna del Rio (GPR)
C. gallica (cn = 54-57)
San Pedro Alcantara (GSP)
C. gallica (cn = 54-57)
C. gallica (cn = 54-57)
C. gallica (cn = 54-57)
C. gallica (cn = 54-57)
Rio Torto (GRT)
C. gallica (cn = 54-57)
C. gallica (cn = 54-57)
Bacillus grandii grandii
Bacillus atticus atticus
Bacillus rossius redtenbacheri
To better unravel haplotype relationships in such a low variability framework, we applied the Templeton's network, which has already proved useful in such situations ( and references therein). The network (Figure 2B) showed that: i) all amphygonic specimens from Tetouan (TET; C. felicitatis) cluster together and show only a little variability (green); ii) as above, two separate clusters include most, but not all, European C. gallica (black); iii) all but one (TAR50) specimens from Targuist are still joined and they all share the same haplotype, regardless of their karyotype; iv) the rest of the haplotypes form a quite homogeneous group, with C. gallica and C. soumiae mixed together, and with only TAF3, TAF4 and SEF42 being different for one substitution.
For AFLPs, the three used highly polymorphic primer combinations (see 'Methods') detected a total of 195 markers for the 27 analyzed individuals. Compared to cox2, AFLP markers show a higher level of variability and enable better differentiation among Clonopsis populations.
The genetic structure obtained by Bayesian analysis (STRUCTURE software) gave additional clues regarding the genetic diversification in Clonopsis. The graph is reported on Figure 3B, aligned to the ME tree for easier comparison. Five replicates for each value of K (from 1 to 12) were run under the admixture model with a burn-in period of 50,000 and 750,000 iterations. The admixture model means that individuals may have mixed ancestry. Moreover, this model appears very useful for stick insects, as it can deal with hybrid zones in a natural way. No prior information was used, and all individuals were deemed as diploid, as shown up by karyotypes. A probability of membership q ≥ 80% was chosen to consider a genotype assigned to one population, while a lower-than-threshold probability means that the individual may have different parental populations, and consequently is admixed via hybridization. In order to determine K, the smallest value of the estimated probability of data was chosen, and this value was then compared with the more formal method proposed by . Both methods gave 4 as the most probable value of K, so we can assume that the dataset includes 4 parental populations that are distinguishable on a genetic basis. One includes the single specimen of C. maroccana (TAR6; purple); a second parental population includes the amphigonic individuals from Tetouan (TET, green); a third one the parthenogenetic females from Sefliane (SEF) and a female from Targuist (TAR50) (red), and a fourth one the two males with cn = 53 (TAR43, TAR47; yellow). All other individuals are not assigned with certainty, and therefore are considered of hybrid origin from between two or more parental populations.
It should be noted that the groupings obtained with the Bayesian analysis mirror the results of the Factorial Correspondence Analysis (FCA; see additional file 1); moreover FCA showed that two groups are the most divergent among the analyzed samples (i.e. TET bisexuals and TAR/SEF females). For this reason, we proceeded in our analysis by forcing the software to accept K = 2. Using this sub-optimal setting, the software brings together individuals in two populations only, which are formed by the elements that are most genetically pure and different, and therefore better indicating specimens with admixed genome. Actually, 10 more runs with K = 2 (burn-in 50,000; 100,000 iterations; admixture model, no prior information) were made without C. maroccana (its presence "pushes" the other individuals to the top of the chart, as it assumes an outgroup behavior; see additional file 1). The two parental populations identified with this analysis (data not shown) include on one side the amphigonic C. felicitatis, on the other side the parthenogenetic females from Sefliane (both C. soumiae and C. gallica) and Targuist (C. soumiae); both were assigned to one of the two parental populations with a probability equal or close to 100%. In addition, two of the three parthenogenetic C. gallica from Oued Laou were assigned to the geographically close population of Tetouan (the diploid C. felicitatis, with a probability of just over 80%), while the remaining one (OLA1) is shown to have a hybrid genotype. All the androgenetic males (both cn = 53 and cn = 35) show an admixed genome. Moreover, two C. gallica specimens (TAF3 and TAF4) as well as a single C. soumiae (CHA26) are indeed admixed too.
On the whole, the pattern of admixture is quite puzzling: although most of the specimens do not show up hybrid genomes, in both C. gallica and C. soumiae we found specimens with statistically-supported admixed genomes. Moreover, C. androgenes males are found, indeed, to have admixed genomes at least with K = 2.
To disentangle Clonopsis evolution, we proceeded with mitochondrial and nuclear DNA analysis, with the aim of finding traces of possible hybridization/polyploidization events, as was the case with other analyzed stick insects ( and references therein). Mitochondrial cox2 gene analysis showed extremely low haplotype variability, except for C. maroccana, which was very different from all other sampled Clonopsis, in line with its highly differentiated karyotype. The mtDNA data for the remaining Clonopsis seemed to support a very recent divergence, as they did not allow splitting of the two parthenogens C. gallica and C. soumiae. On the other hand, AFLP markers showed a good genetic differentiation and distinct groups were detected (K = 4; Figure 3B): one is C. maroccana (purple color), thus confirming mtDNA data; another group is the bisexual C. felicitatis (green) which appears to be a well-defined taxon; a third group (red) is formed by specimens of both C. gallica (cn = 54) and C. soumiae (cn = 72), with no relation to the different chromosome number. The other C. gallica and C. soumiae specimens showed quite a variable genetic constitution, with either admixed or non-admixed genotypes. On the whole, C. gallica and C. soumiae parthenogens did not appear to be homogeneous taxa, but rather a mix of strains of polyphyletic origin, either hybrids or not. Moreover, an admixed hybrid origin seemed to be confirmed for C. androgenes: the male with cn = 35 is invariably admixed, while a hybrid origin of cn = 53 males is supported only for K = 2 (data not shown). This is strong evidence that complex cladogenetic events could account for the observed Clonopsis genetic structure.
When trying to describe Clonopsis evolution, there is a preliminary observation to make: as already mentioned, C. felicitatis, C. gallica and C. soumiae seem to be a reasonable polyploid series with n = 18, i.e. they all have karyotypes that are exact multiples of 18 chromosomes (36 for C. felicitatis, 54 for C. gallica and 72 for C. soumiae). This would be hard to explain without hypothesizing that polyploidization events originated parthenogenetic C. gallica and C. soumiae strains, since it would be extremely odd to imagine that parthenogenetic forms, with karyotypes that are the exact multiple of the closest bisexual species, could have formed other than through polyploidy. Moreover, in stick insects the haploid chromosome number generally ranges from 16 to 20 . For the above mentioned reasons, we feel confident in assuming that polyploidization might have had a major role in Clonopsis evolution, as in that of many other stick insects.
Increases in ploidy level can be achieved by means of several mechanisms during gametogenesis (i.e. pre-meiotic, intra-meiotic or post-meiotic restitution). Invariably, the outcome of these mechanisms is the production of diploid gametes, which, after fertilization, would increase the ploidy of the progeny. Such mechanisms may also include some meiosis (automixis) or not (apomixis), and have already been experimentally confirmed in several complexes . In any case, whenever these mechanisms were confirmed, a clear polyploid karyotype would be recovered.
However, as mentioned before, C. gallica and C. soumiae look morphologically diploid on careful analysis of their karyotypes: actually, although most chromosomes are quite similar, at least some of the biggest cannot be arranged in triplets or quadruplets (see  for detailed pictures of Clonopsis karyotypes). As a consequence, if we accept that both C. gallica and C. soumiae strains are polyploids with diploid karyotypes, then they must have experienced large genome restructuring events, leading to diploidization.
Diploidization of polyploid genomes has been observed in autopolyploids and, most commonly, in allopolyploids. However, despite the increasing evidence of polyploidization as a major force in evolution, the molecular basis of diploidization is far from being fully understood, although many mechanisms have been suggested to date. For instance, tetraploid salmonids are the best-documented case of animal diploidization in autopolyploids: the process proposed took a long time and seems to be still in progress, since it is suggested that it started when, or shortly after, the family originated about 25-100 Mya . This certainly seems not to be the case of Clonopsis, because its low mtDNA variability appears to be an indication of a recent origin of the parthenogenetic strains; therefore, a much quicker diploidization process has to be hypothesized.
Diploidization has been commonly related to hybridization events, followed by a massive rearrangement of the genome . The process, as summarized in , might be as follows: allopolyploids may arise by hybridization of two individuals whose chromosomes (the so-called homoeologues) have similar gene order, but differ in repetitive DNA content (such as in closely-related species or races); after hybridization, homoeologues can go through the loss or gain of genes and repetitive sequences, as well as structural chromosome translocations, thus increasing their morphological divergence. Actually, the extent of structural rearrangements and sequence elimination may vary: the more extensive the rearrangements are, the more distinct the chromosomes will be, so that if the distinctions become extensive enough the species will effectively gain a diploid set.
In more detail, data from  on non-coding sequences suggest a faster way to diploidization, in which a quick DNA elimination, just after polyploidization, takes place: they found that specific sequences named CSSs (Chromosome-Specific Sequences) and GSSs (Genome-Specific Sequences) are eliminated, and suggested a regulatory role for such sequences in the physical chromosome behavior. This leads to the conclusion that the appearance of new polyploid species may be followed by deep genomic changes in a short time, and polyploidization may be an accelerating evolutionary factor itself ; indeed, the finding that one genome can eliminate up to 14% of its loci in a single generation shows that allopolyploidy may lead to the establishment of a new species in one step, and that large-scale genomic rearrangements can occur very quickly .
Might this be the case with Clonopsis? Compared to autopolyploidization, allopolyploidization is a revolutionary event generating two genomic "shocks" in the newly-formed individual, namely hybridity and polyploidy: the former implies that two different genomes are brought together in the same nucleus, the latter results in duplicated genomes. Consequently, the genomes undergo a series of irreversible reorganizations, like structural re-patterning of chromosomes , changes at sequence level, regulation of gene expression, activation of transposons , and amplification, re-assortment or elimination of highly repetitive sequences and low copy sequences . It is reasonable to deduce that epigenetic modifications between genomes may contribute to homologous chromosome recognition and cytological diploidization .
In most cases, the loss of DNA in allopolyploids is unidirectional, with the elimination of fragments from one parental genome only ; incidentally, if applied to Clonopsis parthenogens, this would explain why AFLP markers have lost most (but not all) traces of the hybridizations leading to C. gallica and C. soumiae strains.
However, the main force that drives karyotype diploidization is its higher fitness, because diploidization solves conflicts in the hybrid genome, as well as pairing problems during meiosis. In fact, most of the known diploidized hybrids so far retain meiosis [28–30, 33, 34]. This seems not to be completely true for the parthenogenetic C. gallica and C. soumiae: in fact, in C. gallica time-scheduled investigations on laid eggs  revealed that both European and Moroccan specimens reproduce by apomictic parthenogenesis, albeit of two different kinds, i.e. a meiotic-like mode with two divisions (likely entraining an intra-meiotic structural chromosome doubling) is realized in European specimens of C. gallica, while a unique mitosis is required to allow embryo onset in Moroccan C. gallica. Like Moroccan C. gallica, C. soumiae is invariably maturing eggs through a unique mitosis. Therefore, even though some meiotic features are still retained in some strains, most Clonopsis make use of mitosis to produce their parthenogenetic progeny. So, at present, a diploid karyotype seems not to be a significant advantage for Clonopsis. We can still speculate that all Clonopsis hybrids retained some meiosis at the very beginning when they first arose, as happens now in European strains, thus driving fast diploidization, but it seems hard to explain why some strains, once diploidized, soon after lost their meiosis, as should have happened in North African Clonopsis. We also tested the specimens for the presence of sex-distorting bacteria, such as Rickettsiales , that might have induced parthenogenesis, but we had no evidence for their presence in Clonopsis (data not shown).
Reconstructing Clonopsismicro-evolutionary events
As mentioned, pre-meiotic, intra-meiotic or post-meiotic restitution by endomitosis might explain the ploidy increase in Clonopsis. To account for this, we may hypothesize that the first step to Clonopsis parthenogenetic strains might be a diploid hybrid, showing two complete series of chromosomes of two different species. This hybrid may produce diploid gametes as the outcome of one of the above-mentioned mechanisms of altered meiosis. This may explain how C. soumiae originated: in fact, the fusion of two genetically identical diploid hybrid gametes will produce a tetraploid individual, with a diploid-looking karyotype, if the parental chromosomes are different enough. If this is the case, some admixed genome constitution should be easily detectable in C. soumiae, which is not always true, judging from some of our AFLP data (Figure 3). On the other hand, C. gallica is harder to explain: in fact, if we admit its origin through diploid gametes, its triploid number should be achieved only through the fusion of one haploid and one diploid gamete. In this case, however, some chromosomes will be represented once, the others twice, which seems not to be the case of C. gallica. Therefore, we think that the morphologically diploid structure of Clonopsis karyotypes ought to be looked for in a different cause.
First, we have to mention that the genome of such hypothetical triploid females might be either derived from both sperm and egg nuclei (by syngamy), or from sperm nuclei only, via androgenesis. In androgenesis, the embryo nuclear genome originates from either the doubling of a sperm head or the fusion of two (or more) sperm heads, while the egg pronucleus does not contribute to the genome of the embryo . Androgenesis was first shown in stick insects, and afterwards found in several species of freshwater Corbicula clams [38–40], and in the cypress tree Cupressus dupreziana [41, 42]. At this stage we do not have clear-cut data to assess whether the hypothetical triploid female derived via androgenesis or syngamy; however the low genetic differentiation in Clonopsis mtDNA might be taken as an indication that parthenogens arose by androgenesis from the same maternal ancestor (i.e. C. felicitatis), by keeping its mtDNA and embodying nuclear genomes of extinct or still unsampled paternal bisexuals, as observed in Pijnackeria tetraploids .
Whether originating from syngamy or androgenesis, the "triploid intermediate female" could be either hybrid or not (i.e. it may have chromosome sets derived from the same or different parental species or races), although hybridity would better explain the alteration of meiosis and parthenogenetic reproduction. In any case, such triploid females must have had problems in correctly segregating chromosomes, since trivalents are expected to occur during meiosis of oocytes I. However, in most cases, chromosome triplets are likely to segregate in a 2⇔1 way, i.e. 2 chromosomes go to one pole and the third goes to the opposite one, a behavior that has been observed many times in triploids [43, 44]. This generates a vast array of different chromosome segregations in oocytes II. Two of them are particularly interesting. Case A (Figure 4) segregates two complete series of chromosomes into the oocyte II, while the third one ends up in the first polocyte. A cytologically normal second meiotic division follows, and an anaphasic restitution doubles the chromosome number, likely by the suppression of the second polocyte degeneration (i.e. retention of the polar body). Anaphasic restitution is not new to stick insects, and it has also been found in many other parthenogens . As a result of this process, the new egg gets a tetraploid chromosome number, chromosomes in pairs and the karyotype with a diploid look, while its genome constitution is de facto tetraploid. Such an egg will eventually develop into a parthenogenetic female. We suggest that C. soumiae strains (cn = 72) arose directly in this way. In the second scenario, as reported in scheme B (Figure 4), half of the trivalents are segregating 2⇔1, the other half 1⇔2. The resulting oocyte II is therefore aneuploid, i.e. it has half chromosomes represented twice, while the other half once only. As above, a normal second division follows, and an anaphasic restitution produces an egg that has a triploid chromosome number, but again the karyotype looks diploid and the new genome carries either tetraploid or diploid loci. Eggs like these might have produced C. gallica strains (cn = 54).
If this is the process that generated Clonopsis parthenogenetic strains, it is worth noting that their karyotype diploid-look is just the effect of anaphasic restitution, but their genomes still remain largely (C. gallica) or totally (C. soumiae) polyploid. This may also account for the partial or complete suppression of meiosis in these strains, because multivalents may occur in such complex multi-copy genomes experiencing large homology regions between non-homologues. As a matter of fact, this is completely different from the above-mentioned diploidization mechanisms, which are processes that restore meiosis after polyploidization.
Unfortunately, sizes and centromere positions are similar for most Clonopsis chromosomes and it is not easy to spot whether they are two or fourfold by standard karyotyping, while fine banding techniques that would help in this case have still not been developed for stick insects. Moreover, subsequent minor chromosome changes and/or differences in condensation due to epigenetic modifications of chromatin may further blur chromosome morphology. However, many observations still point to the fact that the proposed process might have happened in Clonopsis, since this hypothesis seems to fit very well with the data we have obtained from this molecular analysis. First of all, given that a hypothetical Clonopsis triploid hybrid female may segregate 18 trivalents with all possible 2⇔1 segregations, it is interesting to calculate the percentage of eggs with the A or the B constitutions: 7.63x10-4% of the eggs will be as in case A, while 18.5% will be like B. Therefore, both events are not unlikely and might have happened many times, because a single Clonopsis female lays up to 100 eggs and each population may contain hundreds of females. Moreover, the B segregation scheme is surprisingly common, so that, each time a triploid female does eventually appear, it could easily result in a new C. gallica strain. This fits our data, which clearly support a rich polyphyletic origin of C. gallica parthenogens. Another surprising observation is well explained by this hypothesis: if both C. gallica and C. soumiae strains may arise at the same time even from a single triploid female, then they can be largely identical using AFLP loci even if their karyotypes are different, a finding that we observed in the Sefliane (SEF) population and that is hard to explain with other hypotheses.
We may recall that the full suppression of meiosis in Clonopsis parthenogens may have occurred at a later stage, also because the hypothetical triploid Clonopsis female was possibly a hybrid between races or subspecies, thus having homoeologues in its genome. It is worth noting that homoeologues are not easily detected by AFLP markers, because they mainly differ in repetitive DNA content (i.e. copy number). This could explain why Clonopsis unisexuals do appear, either admixed or not, depending on the overall nucleotide divergence of the homoeologues carried by each "intermediate triploid female" that gave rise to the strains.
It still remains debatable how, among many different combinations resulting from trivalent differential segregation patterns, only cn = 54 and cn = 72 Clonopsis parthenogenetic strains survived: we may suggest that some sort of genome balancing is implied here, which made cn = 54 and 72 strains able to survive better as parthenogens. Moreover, specific epigenetic genome silencing might also be conceivable in balancing the hybrid genome made up of 54 and 72 chromosomes. The complete lack of data on genetic and epigenetic characterizations of phasmids prevents us from addressing this point better.
In conclusion, we here suggest that C. gallica and C. soumiae parthenogens might have arisen many times through "intermediate triploid females" with altered meiosis. The mechanism proposed here explains all the data we have obtained so far, and, quite significantly, its simple process does not require any new ad-hoc cytological mechanism, since all the proposed steps have been observed many times in closely related stick insects. Given the complexity of Clonopsis micro-evolutionary history, the detailed events leading to each strain are not easy to disentangle at the moment, and this would require larger collecting campaigns in Northern Africa and Europe. Moreover, a genome characterization of Clonopsis, which unfortunately is not available, would better support our hypothesis, and a fine FISH hybridizing technique, such as "chromosome painting", would also help in supporting the proposed model. Our micro-evolutionary scenario for Clonopsis needs more in-depth analyses to be tried out, nevertheless we feel that this is a sound "working hypothesis" that merits further study.
Figure 1 shows collection localities, with population acronyms for the new Moroccan samples, and also reports additional locations in Portugal, Spain and Italy from which some reference C. gallica specimens were utilized. North African forms are particularly hard to collect in a pretty unsafe area such as Northern Algeria and the Rif area of Morocco. At any rate, in 2006, we were able to collect in the Rif area, which is probably the spreading centre of Clonopsis. North African sample included Moroccan C. gallica, the bisexual C. felicitatis (cn = 36/35, XX/X0), the all-female C. soumiae (cn = 72), two strains of ameiotic males, C. androgenes-35 and C. androgenes-53, with cn = 35 (X0) or 53 (X0), and a single C. maroccana (cn = 22/21, XX/X0) female, used as outgroup when needed (see below). They were characterized for mitochondrial gene cytochrome oxidase subunit 2 (cox2, partial sequence). North African populations were also analyzed using AFLP. Detailed data are reported in Table 1.
Mitochondrial DNA analysis
Total genomic DNA was extracted using the DNeasy Blood & Tissue Kit (Qiagen). Partial sequence of cox2 was amplified and directly sequenced according to . The primers utilized were TL2-J-3034 and TK-N-3785 . Sequencing covered 639 bp coding for 213 aminoacids of the Cytochrome Oxidase subunit 2 and corresponds to the gene region sequenced in several insect orders . All sequences were aligned with the Clustal algorithm of MEGA 3.1 . A Bayesian analysis was performed using MrBayes 3.1 (20,000,000 generations; ) (Figure 2A). A Templeton's network  was obtained with TCS 1.21  (Figure 2B). Bacillus grandii grandii, Bacillus atticus atticus and Bacillus rossius redtenbacheri were utilized as outgroups in phylogenetic reconstructions based on cox2.
DNA fingerprinting with selectively neutral AFLP markers was produced according to , using EcoRI/TaqI as restriction enzymes. After a preliminary screening, three highly polymorphic primer pairs carrying ACA/AAC, ACA/AAG and ATG/AAC as selective nucleotides were assayed on 100 ng of total genomic DNA. AFLP fragments were separated by electrophoresis on 8% polyacrylamide gels and the polymorphisms were visually scored as dominant markers, coding with 1 the presence and with 0 the absence of the band. Markers with more than 5% of missing data were removed from the definitive dataset.
The genetic relationships at individual level were assessed by the Factorial Correspondence Analysis (FCA), a statistical method enabling analysis and description graphically and synthetically of two-way or multi-way contingency tables. For this, the software GENETIX 4.05 was used  (see additional file 1).
To assess the molecular structure of Moroccan Clonopsis we used a model-based bayesian procedure as implemented in the software STRUCTURE 2.2 [54, 55]. This model enables identification of the K (unknown) populations of individuals, and the probabilistic assignment of each individual to one or several populations if its genotype indicates that it is admixed. The model assumes that the loci are unlinked and at linkage equilibrium. STRUCTURE version 2.2 calculates a logarithmic probability for the data being assigned to a given number of clusters, based on minimizing linkage between clusters, and maximizing linkage within.
A Minimum Evolution tree (ME, Figure 3A) based on AFLP markers was calculated using PAUP 4.0 ; support for each node was obtained using bootstrap (1000 replicates, ). Given the results of cox2, C. maroccana has been used as an outgroup in the AFLP-based tree, since more phylogenetically distant species (such as Bacillus ssp.) would not be easily comparable using AFLP markers, which are more suitable for genetic analyses of population strains or closely related species , and have been proved to be resolving for phylogenetic structure in rapidly evolving systems .
We are grateful to P. Ajmone Marsan and R. Negrini for AFLP analysis, to Professor Soumia Fahd of the Moroccan Abdelmalek Essaâdi, University of Tetouan, and to her students who helped with collecting at night in the dangerous area of Targuist. This work was supported by Italian "Ministero dell'Università e della Ricerca Scientifica" (MIUR) funding and by the "Donazione Canziani" bequest.
- Wolfe KH: Yesterday's polyploids and the mistery of polyploidization. Nat Rev Genet. 2001, 2: 333-341. 10.1038/35072009.View ArticlePubMedGoogle Scholar
- Van de Peer Y, Maere S, Meyer A: The evolutionary significance of ancient genome duplications. Nat Rev Genet. 2009, 10: 725-732. 10.1038/nrg2600.View ArticlePubMedGoogle Scholar
- Scali V, Tinti F, Mantovani B, Marescalchi O: Mate recognition and gamete cytology features allow hybrid species production and evolution in Bacillus Stick-insects. It J Zool. 1995, 62: 59-70. 10.1080/11250009509356052.Google Scholar
- Ghiselli F, Milani L, Scali V, Passamonti M: The Leptynia hispanica species complex (Insecta Phasmida): polyploidy, parthenogenesis, hybridization and more. Mol Ecol. 2007, 16: 4256-4268. 10.1111/j.1365-294X.2007.03471.x.View ArticlePubMedGoogle Scholar
- Milani L, Scali V, Passamonti M: The Clonopsis gallica puzzle: Mendelian species, polyploid parthenogens with karyotype re-diploidization and clonal androgens in Moroccan stick insects. J Zool Syst Evol Res. 2009, 47: 132-140. 10.1111/j.1439-0469.2008.00489.x.View ArticleGoogle Scholar
- Scali V: Metasexual stick insects: model pathways to lo(o)sing sex. Lost sex. Edited by: Schön I, Martens K, Dijk PV. 2009, Dordrecht, Netherlands: Springer scientific publishers, cpt 16: 1-29.Google Scholar
- Mantovani B, Scali V: Hybridogenesis and androgenesis in the stick-insect Bacillus rossius-grandii benazzi (Insecta Phasmatodea). Evolution. 1992, 46: 783-796. 10.2307/2409646.View ArticleGoogle Scholar
- Passamonti M, Mantovani B, Scali V: Phylogeny and karyotype evolution of the Iberian Leptynia attenuata species complex (Insecta Phasmatodea). Mol Phylogenet Evol. 2004, 30: 87-96. 10.1016/S1055-7903(03)00156-8.View ArticlePubMedGoogle Scholar
- Craddock EM: Chromosomal diversity in the Australian Phasmatodea. Aust J Zool. 1972, 20: 445-462. 10.1071/ZO9720445.View ArticleGoogle Scholar
- John B, Rentz DCF, Contreras N: Extensive chromosome variation in the stick insect genus Sipyloidea Brunner von Wattenwyl (Phylliidae: Necrosciinae) within Australia, and descriptions of three new species. Invert Taxonomy. 1987, 1: 603-30.Google Scholar
- Passamonti M, Mantovani B, Scali V: Karyotype and allozyme characterization of the Iberian Leptynia attenuata species complex (Insecta Phasmatodea). Zool Sci. 1999, 16: 675-684. 10.2108/zsj.16.675.View ArticleGoogle Scholar
- White MJD: Animal cytology and evolution. 1973, London: Cambridge University Press, 3Google Scholar
- Scali V, Milani L: New Clonopsis stick insects from Morocco: the amphigonic C. felicitatis sp.n., the parthenogenetic C. soumiae sp.n., and two androgenetic taxa. It J Zool. 2009, 76: 291-305. 10.1080/11250000802649750.View ArticleGoogle Scholar
- Mantovani B, Passamonti M, Scali V: The mitochondrial cytochrome oxidase 2 gene in Bacillus stick insects: ancestry of hybrids, androgenesis and phylogenetic relationship. Mol Phylogenet Evol. 2001, 19: 157-163. 10.1006/mpev.2000.0850.View ArticlePubMedGoogle Scholar
- Vos P, Hogers R, Bleeker M, Reijans M, Van de Lee T, Hornes M, Frijters A, Pot J, Peleman J, Kuiper M, Zabeau M: AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res. 1995, 23: 4407-4414. 10.1093/nar/23.21.4407.PubMed CentralView ArticlePubMedGoogle Scholar
- Bonin A, Ehrich D, Manel S: Statistical analysis of amplified fragment length polymorphism data: a toolbox for molecular ecologists and evolutionists. Mol Ecol. 2007, 16: 3737-3758. 10.1111/j.1365-294X.2007.03435.x.View ArticlePubMedGoogle Scholar
- Nosil P, Egan SP, Funk DJ: Heterogeneous genomic differentiation between walking-stick ecotypes: "isolation by adaptation" and multiple roles for divergent selection. Evolution. 2008, 62 (2): 316-336. 10.1111/j.1558-5646.2007.00299.x.View ArticlePubMedGoogle Scholar
- Maughan PJ, Saghai Maroof MA, Buss GR, Huestis GM: Amplified fragment length polymorphism (AFLP) in soybean: species diversity, inheritance, and near-isogenic line analysis. TAG. 1996, 93: 0040-5752.Google Scholar
- Albertson RC, Markert JA, Danley PD, Kocher TD: Phylogeny of a rapidly evolving clade: the cichlid fishes of Lake Malawi, East Africa. P Natl Acad Sci USA. 1999, 96: 5107-5110. 10.1073/pnas.96.9.5107.View ArticleGoogle Scholar
- Bensch S, Åkesson M: Ten years of AFLP in ecology and evolution: why so few animals?. Mol Ecol. 2005, 14: 2899-2914. 10.1111/j.1365-294X.2005.02655.x.View ArticlePubMedGoogle Scholar
- Albert V, Jonsson B, Bernatchez L: Natural hybrids in Atlantic eels (Anguilla anguilla, A. rostrata): evidence for successful reproduction and fluctuating abundance in space and time. Mol Ecol. 2006, 15: 1903-1916. 10.1111/j.1365-294X.2006.02917.x.View ArticlePubMedGoogle Scholar
- Bensch S, Helbig AJ, Salomon M, Seibold I: Amplified fragment length polymorphism analysis identifies hybrids between two subspecies of warblers. Mol Ecol. 2002, 11: 473-481. 10.1046/j.0962-1083.2001.01455.x.View ArticlePubMedGoogle Scholar
- Evanno G, Regnaut S, Goudet J: Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Mol Ecol. 2005, 14: 2611-2620. 10.1111/j.1365-294X.2005.02553.x.View ArticlePubMedGoogle Scholar
- White MJD: Insect 2: Blattodea, Mantodea, Isoptera, Grylloblattodea, Phasmatodea, Dermaptera and Embioptera. Animal Cytogenetics. Edited by: John B. 1976, Berlin: Borntraeger, 3: 1-75.Google Scholar
- Huges RN: A functional biology of clonal animals. London: Chapman and Hall LtdGoogle Scholar
- Allendorf FW, Thorgaard GH: Tetraploidy and evolution of salmonid fishes. Evolutionary Genetics of Fishes. Edited by: Turner BJ. 1984, New York: Plenum Press, 1-53.View ArticleGoogle Scholar
- Gregory TR, Mable BK: Polyploidy in animals. The Evolution of the Genome. Edited by: Gregory TR. 2005, San Diego: Elsevier, CA: Academic Press, cpt 8: 427-517.View ArticleGoogle Scholar
- Moore G: Meiosis in allopolyploids - the importance of "Teflon" chromosomes. Trends Genet. 2002, 18: 456-463. 10.1016/S0168-9525(02)02730-0.View ArticlePubMedGoogle Scholar
- Feldman M, Liu B, Segal G, Abbo S, Levy AA, Vega JM: Rapid elimination of low-copy DNA sequences in polyploid wheat: a possible mechanism for differentiation of homeologous chromosomes. Genetics. 1997, 147: 1381-1387.PubMed CentralPubMedGoogle Scholar
- Shaked H, Kashkush K, Ozkan H, Feldman M, Levy AA: Sequence elimination and cytosine methylation are rapid and reproducible responses of the genome to wide hybridization and allopolyploidy in wheat. The Plant Cell. 2001, 13: 1749-1759. 10.2307/3871316.PubMed CentralView ArticlePubMedGoogle Scholar
- Leitch IJ, Bennett MD: Polyploidy in angiosperms. Trends Plant Sci. 1997, 2: 470-476. 10.1016/S1360-1385(97)01154-0.View ArticleGoogle Scholar
- Salmon A, Ainouche ML, Wendel JF: Genetic and epigenetic consequences of recent hybridization and polyploidy in Spartina (Poaceae). Mol Ecol. 2005, 14: 1163-1175. 10.1111/j.1365-294X.2005.02488.x.View ArticlePubMedGoogle Scholar
- Ozkan H, Levy AA, Feldman M: Allopolyploidy-induced rapid genome evolution in the wheat (Aegilops-Triticum) group. The Plant Cell. 2001, 13: 1735-1747. 10.2307/3871315.PubMed CentralView ArticlePubMedGoogle Scholar
- Liu B, Wendel JF: Epigenetic phenomena and the evolution of plant allopolyploids. Mol Phylogenet Evol. 2003, 29: 365-379. 10.1016/S1055-7903(03)00213-6.View ArticlePubMedGoogle Scholar
- Moran NA, Mc Cutcheon JP, Nakabachi A: Genomics and Evolution of Heritable Bacterial Symbionts. Annu Rev Genet. 2008, 42: 165-190. 10.1146/annurev.genet.41.110306.130119.View ArticlePubMedGoogle Scholar
- Scali V, Milani L, Passamonti M: Clonopsis gallica, a stick insect parthenogen exploiting different egg maturation mechanisms over its range. Invertebr Reprod Dev. 2010Google Scholar
- Tinti F, Scali V: Allozymic and cytological evidence for hemiclonal, all-paternal and mosaics offspring of the hybridogenetic stick insect Bacillus rossius-grandii grandii. J Exp Zool. 1995, 273: 149-159. 10.1002/jez.1402730208.View ArticleGoogle Scholar
- Komaru A, Kawagishi T, Konishi K: Cytological evidences of spontaneous androgenesis in the freshwater clam Corbicula leana prime. Dev Genes Evol. 1998, 208: 46-50. 10.1007/s004270050152.View ArticlePubMedGoogle Scholar
- Byrne M, Phelps H, Church T, Adair V, Selvakumaraswamy P, Potts J: Reproduction and development of the freshwater clam Corbicula australis in southeast Australia. Hydrobiologia. 2000, 418: 185-197. 10.1023/A:1003986512832.View ArticleGoogle Scholar
- Qiu A, Shi A, Komaru A: Yellow and brown shell color morphs of Corbicula fluminea (Bivalvia Corbiculidae) from Sichuan Province, China, are triploids and tetraploids. J Shellfish Res. 2001, 20: 323-328.Google Scholar
- Pichot C, El Maâtaoui M, Raddi S, Raddi P: Surrogate mother for endangered Cupressus. Nature. 2001, 412: 39-10.1038/35083687.View ArticlePubMedGoogle Scholar
- McKone MJ, Halpern SL: The evolution of androgenesis. Am Nat. 2003, 161: 641-656. 10.1086/368291.View ArticlePubMedGoogle Scholar
- White MJD: Modes of Speciation. 1978, W.H. Freeman & CoGoogle Scholar
- Marescalchi O, Scali V: Automictic parthenogenesis in the diploid-triploid stick insect Bacillus atticus and its flexibility leading to heterospecific diploid hybrids. Inv Repr Dev. 2003, 43: 163-172.View ArticleGoogle Scholar
- Suomalainen E, Saura A, Lokki J: Cytology and evolution in parthenogenesis. 1987, Boca Raton, Florida: CRC PressGoogle Scholar
- Simon C, Frati F, Beckenbach A, Crespi B, Liu H, Flook P: Evolution, weighting and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers. Ann Entomol Soc Am. 1994, 87: 651-701.View ArticleGoogle Scholar
- Liu H, Beckenbach AT: Evolution of the mitochondrial cytochrome oxidase 2 gene among 10 orders of insects. Mol Phylogenet Evol. 1992, 1: 41-52. 10.1016/1055-7903(92)90034-E.View ArticlePubMedGoogle Scholar
- Kumar S, Tamura K, Nei M: MEGA3: integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief Bioinform. 2004, 5: 150-163. 10.1093/bib/5.2.150.View ArticlePubMedGoogle Scholar
- Huelsenbeck JP, Ronquist F: MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003, 19: 1572-1574. 10.1093/bioinformatics/btg180.View ArticlePubMedGoogle Scholar
- Templeton NS: The polymerase chain reaction. History, methods, and applications. Diagn Mol Pathol. 1992, 1: 58-72. 10.1097/00019606-199203000-00008.View ArticlePubMedGoogle Scholar
- Clement M, Posada D, Crandall KA: TCS: a computer program to estimate gene genealogies. Mol Ecol. 2000, 9: 1657-1659. 10.1046/j.1365-294x.2000.01020.x.View ArticlePubMedGoogle Scholar
- Ajmone Marsan P, Valentini A, Cassandro M, Vecchiotti Antaldi G, Bertoni G, Kuiper M: AFLP® markers for DNA fingerprinting in cattle. Anim Genet. 1997, 28: 418-426. 10.1111/j.1365-2052.1997.00204.x.View ArticlePubMedGoogle Scholar
- Belkhir K, Borsa P, Chikhi L, Raufaste N, Bonhomme F: GENETIX 4.05, Population genetics software for Windows TM. 2004, Laboratoire Génome, Populations, Interactions, CNRS UMR 5000, Université de Montpellier II, Montpellier, FranceGoogle Scholar
- Pritchard JK, Stephens M, Donnelly P: Inference of population structure using multilocus genotype data. Genetics. 2000, 155: 945-959.PubMed CentralPubMedGoogle Scholar
- Falush D, Stephens M, Pritchard JK: Inference of population structure using multilocus genotype data: dominant markers and null alleles. Mol Ecol Notes. 2007, 7: 574-578. 10.1111/j.1471-8286.2007.01758.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Swofford DL: PAUP*. Phylogenetic Analysis Using Parsimony (*and other methods), version 4. 2003, Sinauer & Associates, Sunderland MassachusettsGoogle Scholar
- Felsenstein J: Confidence limits on phylogenies: an approach using the bootstrap. Evolution. 1985, 39: 783-791. 10.2307/2408678.View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.